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临床试验/JPRN-UMIN000003113
JPRN-UMIN000003113已完成1 期

Combination chemotherapy of hepatic arterial infusion chemotherapy with cisplatin and S-1in patients with advanced hepatocellular carcinoma: phase I trial - Phase I trial of CDDP-HAI+S-1 in advanced HCC

ational Cancer Center0 个研究点目标入组 25 人开始时间: 2010年2月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Prior chemotherapy with cisplatin and fluorouracil for hepatocellular carcinoma 2) Prior radiotherapy, transcatheter arterial chemoembolization, and hepatic arterial chemotherapy for portal vein tumor thrombosis of hepatocellular carcinoma 3) Refractory pleural effusion or ascites 4) Distant metastases 5) Allergic reaction to iodine contrast material 6) Severe renal disease 7) Severe heart disease 8) Active infection excluding hepatitis B or C viral infection 9) Active concomitant malignancy 10) Severe mental disorder 11) Severe allergic reaction to drug 12) Pregnant and lactating females; females of childbearing age unless using effective contraception

研究者

发起方
ational Cancer Center

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